A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979807



Internal ID22754742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33158747..33171455hg38UCSC Ensembl
chr19:33649653..33662361hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3812709
hg1912709
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17394010
Samples
Known GenesWDR88
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979807
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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